Clearance Summary
CHOLESTRAK HDL CHOLESTEROL HOME TEST received FDA 510(k) clearance under submission number K072836, sponsored by Accutech, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2007-12-27.
- Submission: K072836
- Applicant / Sponsor: Accutech, LLC
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1475
- Decision date: 2007-12-27
Classification & Regulation
This clearance is catalogued under FDA product code LBS and 21 CFR 862.1475, within the Clinical Chemistry review panel as a Class I device.